Canonical Allele Identifier: PA2829531059
Gene: KCNQ2 HGNC NCBI

Linked Data

ClinVar Variation Id: 999695
ClinVar RCV Id: RCV001295719

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004509.2:p.Ala423Val
CA9958466
NM_004518.5:c.1268C>T